FDA Devices recall · Reported August 19, 2026
Brand Name: Xhibit Product Name: Xhibit Central Station Model/Catalog Number: 96102 Software Version: N/A Product Description: The Spacelabs Healthcare (Spacelabs) Xhibit Central Station, Model 96102. Xhibit offers remote surveillance of patient data for those patients connected to a Spacelabs Healthcare bedside monitors and telemetry systems. The DisplayPort audio/video splitter allows users to extend the audio/video source from the Xhibit to additional external displays or monitors. This e
Due to off-the-shelf display port component that has audio/video failures
Spacelabs Healthcare, Inc. recalled Brand Name: Xhibit Product Name: Xhibit Central Station Model/Catalog Number: 96102 So… - a moderate-severity action.
Brand Name: Xhibit Product Name: Xhibit Central Station Model/Catalog Number: 96102 So… was recalled by Spacelabs Healthcare, Inc. in August 19, 2026. Reason: Due to off-the-shelf display port component that has audio/video failures. Check the official notice for the remedy. Verify recall #Z-2916-2026 with the FDA Devices before acting.
The recall
Spacelabs Healthcare, Inc. issued this moderate-severity FDA Devices recall-Due to off-the-shelf display port component that has audio/video failures.
- Moderate
- severity level
- 6K units
- affected scope
- Class II
- classification
- August 19, 2026
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2916-2026 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2916-2026) was formally reported on August 19, 2026, with the manufacturer initiating the action on June 4, 2026. It is classified under Moderate severity (Class II), with a current status of Ongoing. Spacelabs Healthcare, Inc. is listed as the recalling firm, operating out of Snoqualmie, WA. Federal records list the affected scope as 6074.
The documented reason for this recall is: Due to off-the-shelf display port component that has audio/video failures Distribution data in the federal record shows the product reached: Worldwide - US Nationwide distribution in the states of AK, AL, AR, AZ, CA, CO, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX,…. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 41,021 medical devices recalls on record
Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Product description
Brand Name: Xhibit Product Name: Xhibit Central Station Model/Catalog Number: 96102 Software Version: N/A Product Description: The Spacelabs Healthcare (Spacelabs) Xhibit Central Station, Model 96102. Xhibit offers remote surveillance of patient data for those patients connected to a Spacelabs Healthcare bedside monitors and telemetry systems. The DisplayPort audio/video splitter allows users to extend the audio/video source from the Xhibit to additional external displays or monitors. This extension of audio/video is for viewing only and does not allow interaction with the Xhibit. Component: The DisplayPort audio/video splitter is a 3rd party external accessory to Xhibit.
Reason for recall
Due to off-the-shelf display port component that has audio/video failures
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-2916-2026 |
| Date reported | August 19, 2026 |
| Date initiated | June 4, 2026 |
| Recalling firm | Spacelabs Healthcare, Inc. |
| Firm location | Snoqualmie, WA |
| Affected scope | 6074 |
| Distribution | Worldwide - US Nationwide distribution in the states of AK, AL, AR, AZ, CA, CO, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, VA, WA, WI, WY and … |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-2916-2026) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Methodology · Corrections · Archive as of August 2026